Barcode-free single vesicle multiplexed protein and rna analysis

Abstract

According to various embodiments, a system and method for characterizing protein and nucleic acid content of a plurality of individual particles. The method includes encapsulating individual particles into compartments also containing analyte specific binding complements with oligonucleotide tags comprising a unique molecular identifier sequence, a sequence to identify the analyte specific binding complement, and a homology domain sequence. Allowing the oligonucleotide tags to hybridize on homology domain to form initial tag pairs, amplifying the tag pairs, using an enzyme to cut at the homology domain, allowing tags to re-hybridize, pooling the compartments, and sequencing. Finally, predicting co-encapsulated analytes by computational identification of clusters based on more frequently found oligonucleotide tag pairs.

What is claimed is: 
     
         1 . A method for characterizing protein and nucleic acid content of individual particles, the method comprising:
 encapsulating a plurality of particles into compartments, the plurality of particles including nucleic acid sequences, the compartments also containing analyte specific binding complements with oligonucleotide tags, the tags including a sequence to identify the analyte specific binding complement and two unique molecular identifier (UMI) sequences separated by a restriction enzyme cleavage site;   amplifying the tags;   using an enzyme to cut at the restriction site;   allowing cut tags to re-hybridize;   pooling the compartments;   sequencing the nucleic acid sequences of the particles; and   predicting co-encapsulated analytes by computational identification of clusters based on more frequently found UMI pairs.   
     
     
         2 . The method of  claim 1 , wherein the particles are lipid vesicles. 
     
     
         3 . The method of  claim 1 , wherein the oligonucleotide tags include a nucleic acid binding end to bind to nucleic acids associated with the encapsulated individual particle. 
     
     
         4 . The method of  claim 3 , wherein the nucleic acid binding end is a poly-A tail. 
     
     
         5 . The method of  claim 1 , where the compartments are formed by an emulsion. 
     
     
         6 . The method of  claim 1 , wherein the compartments are formed by microfabricated microwells to allow for easier subsequent processing. 
     
     
         7 . The method of  claim 1 , further comprising lysing of the particles if intravesicular nucleotides or analytes need to be accessed. 
     
     
         8 . The method of  claim 7 , wherein lysing vesicles includes injecting a new line of buffer containing exosome lysis reagents into each droplet. 
     
     
         9 . The method of  claim 7  where lysing of vesicles includes a freeze thaw cycle. 
     
     
         10 . The method of  claim 1 , further comprising a cleanup step and purifying step during sequencing. 
     
     
         11 . The method of  claim 2 , wherein encapsulating the plurality of particles includes using one or more of the following: polymer-based precipitation methods, size exclusion chromatography, ultrafiltration, ultracentrifugation, flotation density gradient, microfluidic and immunoaffinity methods. 
     
     
         12 . The method of  claim 5 , wherein encapsulating the plurality of particles includes emulsifying the particles into droplets. 
     
     
         13 . The method of  claim 12 , wherein emulsifying the particles into droplets is achieved using a droplet generator, a home-made microfluidic droplet generating device, or through vigorous shaking. 
     
     
         14 . The method of  claim 1 , wherein the oligonucleotide tags are freed from their analyte specific binding complements includes using light to cleave a photocleavable linker. 
     
     
         15 . The method of  claim 1 , wherein nucleic acids associated with the encapsulated individual particle bind to the oligonucleotide tags and are amplified in subsequent processing steps. 
     
     
         16 . The method of  claim 1 , wherein amplifying the tags includes using overlap extension polymerase chain reaction. 
     
     
         17 . The method of  claim 1 , further comprising deactivating the enzyme with heat thereby allowing re-ligating or re-hybridization of singlets to form pairs within the same compartment. 
     
     
         18 . The method of  claim 1 , wherein pooling is achieved by breaking an emulsion. 
     
     
         19 . The method of  claim 18 , wherein breaking of the emulsion includes using demulsifiers, or using electrostatic pulses. 
     
     
         20 . The method of  claim 1 , wherein an oligonucleotide tag contains a homology domain sequence and separate oligonucleotide tags are allowed to hybridize on the homology domain to form a UMI pair.